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Sphygmomanometer - ANVISA Registration 80686360122

Access comprehensive regulatory information for Sphygmomanometer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80686360122 and manufactured by MDF Instruments Medifriend Inc.. The registration is held by MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including HONSUN (NANTONG) CO. LTD, PRESS CONTROL INDÚSTRIA E COMÉRCIO LTDA - ME, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80686360122
Registration Details
ANVISA Registration Number: 80686360122
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Device Details

Esfigmomanômetro Aneroide MDF
Risk Class II

Registration Details

80686360122

25351425221201601

09117476000181

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Nov 28, 2016

VIGENTE

09/18/2025 19:00:01